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The Associate Director of Drug Product CMC is responsible for leading and overseeing drug product development, manufacturing, and regulatory activities to ensure the delivery of high-quality products from early development through commercialization. This role requires cross-functional collaboration to support product lifecycle management, process optimization, and regulatory compliance, ensuring that all CMC strategies align with company goals and regulatory standards. The position involves providing technical and strategic leadership while working closely with internal teams and external partners to meet critical project milestones.